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Mutation detection of ATP2C1 gene in Chinese patients with Hailey-Hailey disease / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 63-65, 2008.
Article in Chinese | WPRIM | ID: wpr-229819
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the mutations of ATP2C1 gene in Chinese patients with Hailey-Hailey disease (HHD).</p><p><b>METHODS</b>Genomic DNA was extracted from peripheral blood leukocytes. PCR and direct DNA sequencing were used to detect the mutations in all 27 exons of ATP2C1 gene in patients of two Chinese families and a sporadic patient with HHD.</p><p><b>RESULTS</b>Three mutations in ATP2C1 gene were found, including 1 nonsense mutation, 1 deletion/frameshift mutation and 1 missense mutation. All of them were novel mutations.</p><p><b>CONCLUSION</b>All the three mutations could affect the transcription and translation, and further the function of protein encoded by ATP2C1 gene.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pedigree / DNA Mutational Analysis / Base Sequence / Case-Control Studies / Exons / Sequence Alignment / Pemphigus, Benign Familial / Sequence Deletion / Calcium-Transporting ATPases / Codon, Nonsense Type of study: Diagnostic study / Observational study Limits: Adult / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2008 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pedigree / DNA Mutational Analysis / Base Sequence / Case-Control Studies / Exons / Sequence Alignment / Pemphigus, Benign Familial / Sequence Deletion / Calcium-Transporting ATPases / Codon, Nonsense Type of study: Diagnostic study / Observational study Limits: Adult / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2008 Type: Article